Osteomyelitis of the hip in a child

Clinical Cases 29.01.2010
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Section: Musculoskeletal system
Case Type: Clinical Cases
Patient: 5 years, male
Authors: Formicola A, Marchetti M, Di Giambattista A, Arena C, Rossi M, Bargellini I, Bartolozzi C.
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AI Report

Clinical History

The patient was pyrexial with a temperature of 39°C and complaining of lower limbs pain predominantly at the right knee and at the right hip joint. He had suffered multiple events of otitis and tonsillitis.

Imaging Findings

A 5 year old boy presented with fever (39°C) and lower limbs pain predominantly at the right knee and hip joint. Two weeks before he had a sore throat, cough and rhinitis.
He had raised inflammatory markers: laboratory result demonstrated an increase of ESR and C-reactive protein and a neutrophilic leukocytosis. The patient had a limp and a physical examination revealed a narrow range of right hip movements.
He underwent an ultrasound (US) exam of the hips that revealed a moderate intra-articular fluid collection, without capsular and synovial thickening (Fig 1). These findings suggested a diagnosis of transient hip synovitis.
Two weeks after an anti-inflammatory therapy he showed pain relief. However, at US exam the intra-articular effusion persisted. Magnetic Resonance (MR) scan of the hip showed an area of bone marrow oedema in the acetabulum, with moderate edema of the surrounding soft tissues (Fig 2).
A plain film radiography of the hip was normal (Fig 3). These abnormalities suggested the diagnosis of osteomyelitis, supported by clinical signs and symptoms.
He was given parenteral antibiotics associated with anti-inflammatory therapy.
A month later, MR revealed a reduction of acetabular bone marrow involvement and soft tissue oedema (Fig 4); the therapy was therefore continued. At two months’ follow-up MR did not show any radiological abnormality (Figure 5) and patient was symptom free.

Discussion

Acute haematogenous osteomyelitis (AHO) is a common paediatric problem. It is an inflammation of bone and bone marrow, usually caused by bacterial infections (most frequently S. aureus).
In children it typically occurs in long tubular bones. Involvement of pelvic bones is relatively rare (6.3-20%).
Early diagnosis prevents sepsis, chronic infection, growth arrest, and deforming bone damage. Unfortunately, diagnosis can be difficult.
Infections in neonates and infants are initially clinically silent. Young children may present with only limping or refusal to bear weight. In pelvic infection, irritation of the lumbosacral plexus can mimic lumbar disk disease, and extension into the iliac fossa can produce abdominal pain.
Screening laboratory studies often lack of specificity and sensitivity. ESR is the best laboratory test, but positive predictive value is <26%. Blood cultures can only be positive if there is bacteremia.
When AHO is suspected, plain-film radiography, as initial imaging test, can show soft-tissue swelling as early as 48 h after the onset of symptoms but shows bone destruction or periosteal reaction only after 7–10 days, whereas lytic changes are more delayed, requiring 50-75% bone destruction.
US represents an appealing, expeditious imaging modality for screening of paediatric patients with clinically suspected osteomyelitis. It may shows fluid collections contiguous to the bone, suggestive of osteomyelitis. US should then be followed by other imaging techniques.
Computed tomography (CT) may play a role in the diagnosis of osteomyelitis, showing increased bone-marrow density and, in certain instances, intramedullary gas and depicting soft tissue involvement. CT may also demonstrate areas of necrotic bone.
Skeletal scintigraphy has played a central role in expediting diagnosis. Its sensitivity and specificity exceed 90% when it is interpreted with knowledge of clinical findings. It seldom requires sedation and provides a whole-body survey, which is useful when symptoms are poorly localized and when AHO is multifocal, as occurs in about 6% of paediatric cases .The difficulty in separating bone-marrow processes from soft-tissue disease limits specificity and accuracy.
MR is a valid imaging modality, able to confirm and localize the infection or establish an alternative diagnosis. Reported sensitivity and specifity in the diagnosis of osteomyelitis range between 88-100% and 75-100%, respectively.
Compared to scintigraphy, MR can differentiate between bone and soft-tissue infections; however, whole-body examinations are not feasible.
Criteria for diagnosis of acute osteomyelitis are decreased marrow signal intensity on T1-weighted images and corresponding increased signal intensity on short-tau inversion-recovery (STIR) images or normal to increased signal intensity on T2-weighted spin-echo (SE) images because of oedema, hyperemia, and exudate. The combination of T1-weighted and T2-weighted images is essential to distinguish abscesses and fluid collections.
In conclusion, plain radiographs represent the initial imaging test. US is particularly indicated in paediatric patients. MR should be requested to confirm the diagnosis and define site and extension of the disease. If MR is not feasible or when symptoms are poorly localized, bone scintigraphy (ideally, leukocyte scans for acute osteomyelitis and technetium scans for chronic osteomyelitis) should be performed.

Differential Diagnosis List

Osteomyelitis of the hip

Final Diagnosis

Osteomyelitis of the hip

Liscense

Figures

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Plain-film radiography

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Plain-film radiography

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